Evidence map›Paper›PMID 31995593›Full record

ArticlePloS one2020

Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach.

Tripti Agarwal, Tanica Lyngdoh, Frank Dudbridge, Giriraj Ratan Chandak, Sanjay Kinra, Dorairaj Prabhakaran, K Srinath Reddy, Caroline L Relton, George Davey Smith, Shah Ebrahim and 2 more

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Tripti AgarwalIndian Institute of Public Health-Delhi, Public Health Foundation of India, Gurgaon, India.
Tanica LyngdohIndian Institute of Public Health-Delhi, Public Health Foundation of India, Gurgaon, India.
Frank DudbridgeDepartment of Health Sciences, University of Leicester, Leicester, United Kingdom.
Giriraj Ratan ChandakCSIR-Centre for Cellular and Molecular Biology, Hyderabad, India.ORCID 0000-0002-3095-9453
Sanjay KinraDepartment of Non-Communicable Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0001-6690-4625
Dorairaj PrabhakaranPublic Health Foundation of India, Gurgaon, India.
K Srinath ReddyPublic Health Foundation of India, Gurgaon, India.
Caroline L ReltonMRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
George Davey SmithMRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, United Kingdom.ORCID 0000-0002-1407-8314
Shah EbrahimDepartment of Non-Communicable Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Vipin GuptaDepartment of Anthropology, University of Delhi, Delhi, India.
Gagandeep Kaur WaliaPublic Health Foundation of India, Gurgaon, India.ORCID 0000-0001-8081-2284

Funding

Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_00011/5Medical Research Council MC_UU_12013/2Wellcome TrustWellcome Trust 083541/Z/07/ZWellcome Trust GR070797MF
6 · The paper itself

Abstract

backgroundDyslipidemia and abnormal glycemic traits are leading causes of morbidity and mortality. Although the association between the two traits is well established, there still exists a gap in the evidence for the direction of causality.

objectiveThis study aimed to examine the direction of the causal relationship between lipids and glycemic traits in an Indian population using bidirectional Mendelian randomization (BMR).

methodsThe BMR analysis was conducted on 4900 individuals (2450 sib-pairs) from the Indian Migration Study. Instrument variables were generated for each lipid and glycemic trait (fasting insulin, fasting glucose, HOMA-IR, HOMA-β, LDL-cholesterol, HDL-cholesterol, total cholesterol and triglycerides) to examine the causal relationship by applying two-stage least squares (2SLS) regression in both directions.

resultsLipid and glycemic traits were found to be associated observationally, however, results from 2SLS showed that only triglycerides, defined by weighted genetic risk score (wGRS) of 3 SNPs (rs662799 at APOAV, rs780094 at GCKR and rs4420638 at APOE/C1/C4), were observed to be causally effecting 1.15% variation in HOMA-IR (SE = 0.22, P = 0.010), 1.53% in HOMA- β (SE = 0.21, P = 0.001) and 1.18% in fasting insulin (SE = 0.23, P = 0.009). No evidence for a causal effect was observed in the reverse direction or between any other lipid and glycemic traits.

conclusionThe study findings suggest that triglycerides may causally impact various glycemic traits. However, the findings need to be replicated in larger studies.

Indexed as

Quantitative Trait, HeritableAdultBlood GlucoseCholesterolCholesterol, HDLCholesterol, LDLCross-Sectional StudiesFemaleGenotyping TechniquesHumansIndiaInsulinInsulin ResistanceLeast-Squares AnalysisLipidsMaleBlood GlucoseCholesterolCholesterol, HDLCholesterol, LDLInsulinLipidsTriglycerides

Identifiers

PMID31995593
PMCPMC6988960

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.